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Analysis of Postoperative Bandage Use Protocols in Otoplasty

Analysis of the Influence of Different Protocols of Postoperative Elastic Bandage Use in the Results of Otoplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01810497
Enrollment
70
Registered
2013-03-13
Start date
2012-05-31
Completion date
2015-03-31
Last updated
2015-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prominent Ears

Keywords

External ear, Ear abnormalities, External ear cartilages

Brief summary

The aim of the study is to investigate the possible influence of different durations of use of postoperative elastic bandaging (seven days vs. thirty days) in the results of otoplasty. We hypothesize that the duration of elastic bandage use has no significant influence on the incidence of relapse of prominence of the ears and need for reoperation.

Interventions

PROCEDUREUse of ear bandage

Elastic bandage to be used on the postoperative period of otoplasty, starting immediately after the procedure. To be used 24hours/day for the specified period.

Sponsors

University of Campinas, Brazil
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
10 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Congenital bilateral ear prominence * 10 years-old or older * No previous attempt of surgical treatment

Exclusion criteria

* Pregnant women * Breastfeeding women * Blod clotting disorders or current anticoagulant use * Uncontrolled systemic diseases

Design outcomes

Primary

MeasureTime frame
Incidence of re-operationuntil 12 months

Secondary

MeasureTime frame
Change from immediate postoperative period of helix-mastoid distance6 months

Other

MeasureTime frame
Incidence of hemorrhagic complications1 month

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026